PRMT6 associates with LEF1 to enhance LEF1/beta-catenin transcriptional activity

碩士 === 國立臺灣大學 === 分子醫學研究所 === 93 === Wnt signals control developmental processes and its deregulation leads to various cancers. Wnt molecules transduce signals through beta-catenin/LEFs(LEF1, TCF4 and its homologs). Upon wnt signaling, beta-catenin accumulates and associates with LEFs to transactiv...

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Main Authors: Chi-Yan Hsiao, 蕭積晏
Other Authors: 林陽生
Format: Others
Language:en_US
Published: 2004
Online Access:http://ndltd.ncl.edu.tw/handle/97839407792241116322
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spelling ndltd-TW-093NTU055380172015-10-13T11:12:50Z http://ndltd.ncl.edu.tw/handle/97839407792241116322 PRMT6 associates with LEF1 to enhance LEF1/beta-catenin transcriptional activity 精氨酸甲基化酵素-6與林巴促進因子結合以增強基因活化之研究 Chi-Yan Hsiao 蕭積晏 碩士 國立臺灣大學 分子醫學研究所 93 Wnt signals control developmental processes and its deregulation leads to various cancers. Wnt molecules transduce signals through beta-catenin/LEFs(LEF1, TCF4 and its homologs). Upon wnt signaling, beta-catenin accumulates and associates with LEFs to transactivate specific genes. LEFs are required for body plan formation, cell fate determination, cells proliferation and survival. It was well known that various proteins, such as CBP, HDAC, PIAS, and Groucho-related proteins, participated in LEFs/beta-catenin transcriptional activity. Here, we performed yeast two-hybrid screening through fetal brain libraray and mammary gland library to search additional proteins involved in LEFs/beta-catenin transcriptional activity. PRMT6 was identified to interact with LEF1 both in vivo and in vitro. It was also shown to enhance LEF1/beta-catenin transcriptional activity on reporter assay. 林陽生 2004 學位論文 ; thesis 40 en_US
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language en_US
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description 碩士 === 國立臺灣大學 === 分子醫學研究所 === 93 === Wnt signals control developmental processes and its deregulation leads to various cancers. Wnt molecules transduce signals through beta-catenin/LEFs(LEF1, TCF4 and its homologs). Upon wnt signaling, beta-catenin accumulates and associates with LEFs to transactivate specific genes. LEFs are required for body plan formation, cell fate determination, cells proliferation and survival. It was well known that various proteins, such as CBP, HDAC, PIAS, and Groucho-related proteins, participated in LEFs/beta-catenin transcriptional activity. Here, we performed yeast two-hybrid screening through fetal brain libraray and mammary gland library to search additional proteins involved in LEFs/beta-catenin transcriptional activity. PRMT6 was identified to interact with LEF1 both in vivo and in vitro. It was also shown to enhance LEF1/beta-catenin transcriptional activity on reporter assay.
author2 林陽生
author_facet 林陽生
Chi-Yan Hsiao
蕭積晏
author Chi-Yan Hsiao
蕭積晏
spellingShingle Chi-Yan Hsiao
蕭積晏
PRMT6 associates with LEF1 to enhance LEF1/beta-catenin transcriptional activity
author_sort Chi-Yan Hsiao
title PRMT6 associates with LEF1 to enhance LEF1/beta-catenin transcriptional activity
title_short PRMT6 associates with LEF1 to enhance LEF1/beta-catenin transcriptional activity
title_full PRMT6 associates with LEF1 to enhance LEF1/beta-catenin transcriptional activity
title_fullStr PRMT6 associates with LEF1 to enhance LEF1/beta-catenin transcriptional activity
title_full_unstemmed PRMT6 associates with LEF1 to enhance LEF1/beta-catenin transcriptional activity
title_sort prmt6 associates with lef1 to enhance lef1/beta-catenin transcriptional activity
publishDate 2004
url http://ndltd.ncl.edu.tw/handle/97839407792241116322
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